Mencylate
- Product NDC
- 59088-215
- 11-digit product format
- 590880215
- Labeler code
- 59088
- Product ID
- 59088-215_23734cfb-47fb-fb71-e063-6394a90a85de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol, Methyl Salicylate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-03-24
- Substance
- MENTHOL; METHYL SALICYLATE
- Active strength
- 20; 100 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mencylate
- Brand name suffix
- Pain Relieving
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 20 mg/mL |
| METHYL SALICYLATE | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A, LAV5U5022Y |
| Rxcui | 311503 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-215-05 | MencylatePain Relieving | 59 mL in 1 JAR | CREAM | 59 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-215 | MENCYLATE PAIN RELIEVING (MENTHOL, METHYL SALICYLATE) CREAM [PURETEK CORPORATION] | 3 | Current NDC, 1 package rows | 20241004_f824de86-9492-2e6b-e053-6294a90a6f2a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59088-215-05 | 59088021505 | 59 mL in 1 JAR (59088-215-05) | 59 ml | 2023-03-24 | No | No | Historical |